Evidence map›Paper›PMID 42709872›Full record

ArticlePLoS computational biology2026

scGSI: Graph-guided self-supervised integration of paired single-cell multi-omics.

Xiang Chen, Zihan Yang, Xiaoyu Liu, Zhiyi Xie, Wenlu Guo

Abstract read
In one paragraph

Article in PLoS computational biology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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4 · The record

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5 · Who and what money

Authors and funding

5 authors.

Xiang ChenSchool of Computer Science and Engineering, Hunan University of Science and Technology, Xiangtan, Hunan, China.ORCID 0000-0002-4797-8837
Zihan YangSchool of Computer Science and Engineering, Hunan University of Science and Technology, Xiangtan, Hunan, China.ORCID 0009-0005-8421-0965
Xiaoyu LiuSchool of Computer Science and Engineering, Hunan University of Science and Technology, Xiangtan, Hunan, China.
Zhiyi XieSchool of Computer Science and Engineering, Hunan University of Science and Technology, Xiangtan, Hunan, China.
Wenlu GuoSchool of Computer Science and Engineering, Hunan University of Science and Technology, Xiangtan, Hunan, China.

Funding

National Natural Science Foundation of China
6 · The paper itself

Abstract

Paired single-cell multi-omics technologies provide direct within-cell correspondence across molecular layers and offer a powerful route to dissecting cellular heterogeneity and regulatory relationships. However, effective integration requires more than modality mixing: a useful model must accurately align paired cells while preserving modality-specific topological structure and biologically meaningful variation. Existing methods often struggle with topology mismatch across modalities, underuse cross-modal complementarity within paired cells, or improve alignment at the cost of biological fidelity. To address these challenges, we present scGSI, a graph-guided self-supervised framework for paired single-cell multi-omics integration. scGSI combines heterogeneous graph encoders to preserve modality-specific neighborhood structure, a pull-in projection module to stabilize pre-alignment, and a cross-fusion mechanism with contrastive refinement to exploit complementary signals between paired modalities. Across five paired single-cell multi-omics datasets collected from four platforms, scGSI improves paired cell-state alignment while maintaining a favorable balance between modality mixing and biological variation preservation. The learned embeddings also better support downstream analyses, including cell-type discrimination and developmental trajectory inference, showing that accurate alignment need not erase biologically meaningful structure.

Indexed as

Computational BiologyMultiomicsSingle-Cell AnalysisAlgorithmsAnimalsHumans

Identifiers

PMID42709872
PMCPMC13577519

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.